Reduced-pressure wound dressings

ABSTRACT

Systems, methods, and dressings for treating a linear wound, such as an incision, on a patient are presented. The systems, dressings, and methods involve a sealed wound dressing assembly that helps form a fluid seal around the linear wound while simultaneously encompassing a subcutaneous delivery conduit to deliver fluid to or from a subcutaneous tissue site. In one instance, a reduced-pressure interface is used to allow the subcutaneous delivery conduit to pass through tissue at or near the linear wound and through a wound dressing assembly to a drainage receptacle.

RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.14/656,439, entitled “Reduced-Pressure Wound Dressings,” filed Mar. 12,2015, which is a continuation of U.S. patent application Ser. No.13/554,572, entitled “Reduced-Pressure Wound Dressings,” filed Jul. 20,2012, now U.S. Pat. No. 8,992,510, which claims the benefit, under 35USC § 119(e), of the filing of U.S. Provisional Patent Application Ser.No. 61/514,801, entitled “Reduced-Pressure Wound Dressings,” filed Aug.3, 2011, all of which are incorporated herein by reference for allpurposes.

BACKGROUND

The present disclosure relates generally to medical treatment systemsand, more particularly, but not by way of limitation, toreduced-pressure dressings having a drain adapter and related systems,and methods for treating incisions.

Clinical studies and practice have shown that providing a reducedpressure in proximity to a tissue site can augment and accelerate thegrowth of new tissue at the tissue site. The applications of thisphenomenon are numerous, but application of reduced pressure has beenparticularly successful in treating wounds. This treatment (frequentlyreferred to in the medical community as “negative pressure woundtherapy,” “reduced-pressure therapy,” or “vacuum therapy”) provides anumber of benefits, which may include faster healing and increasedformulation of granulation tissue. Typically, reduced pressure isapplied to tissue through a wound dressing assembly that includes aporous pad or other manifold device. The porous pad distributes reducedpressure to the tissue and channels fluids that are drawn from thetissue.

SUMMARY

According to an illustrative embodiment, a reduced-pressure system fortreating a tissue site having a linear wound includes a dressing bolsterformed from a medical bolster material. The dressing bolster is forplacing on a patient's epidermis and is substantially sized to overlaythe linear wound. The system further includes an over-drape forproviding a fluid seal over the dressing bolster and a portion of thepatient's epidermis, a reduced-pressure source, and a firstreduced-pressure interface fluidly coupled to the dressing bolster andthe reduced-pressure source. The first reduced-pressure interface is fordelivering reduced pressure to the dressing bolster. The system alsoincludes a reduced-pressure delivery conduit for fluidly coupling thereduced-pressure source and the first reduced-pressure interface. Thesystem further includes a second reduced-pressure interface coupled tothe over-drape, wherein the second reduced-pressure interface is sizedand configured to receive a subcutaneous delivery conduit and to form afluid seal about the subcutaneous delivery conduit.

According to another illustrative embodiment, a wound dressing assemblyfor treating a tissue site having a linear wound includes a dressingbolster having a first surface and a second, inward facing surface fordeploying over a patient's epidermis and substantially sized to overlaythe linear wound; an over-drape for providing a fluid seal over thedressing bolster and a portion of the patient's epidermis; and a firstreduced-pressure interface operable to receive a reduced-pressure supplyconduit. The assembly further includes an inner layer having a firstsurface and a second, inward-facing surface, and formed within atreatment-area aperture. The first surface of the inner layer is coupledat least in part to the second surface of the dressing bolster. Asecond-reduced-pressure interface includes an interface body formed withan aperture and having a first side and a second, patient-facing side.The aperture is sized to receive a subcutaneous delivery conduit and toform a fluid seal therewith. The second reduced-pressure interface isadapted to allow the subcutaneous delivery conduit to pass from asubcutaneous tissue site to an external site through the aperture. Thesubcutaneous delivery conduit is routed through the treatment-areaaperture and the dressing bolster to the second interface.

According to another illustrative embodiment, a method of treating atissue site having a linear wound includes applying a wound dressingassembly to the tissue site. The wound dressing assembly includes adressing bolster formed from a medical bolster material that is shapedfor placing on a patient's epidermis and substantially sized to overlaythe linear wound, an over-drape for providing a fluid seal over thedressing bolster and a portion of the patient's epidermis, a firstreduced-pressure interface fluidly coupled to the dressing bolster fordelivering reduced-pressure to the dressing bolster, and a secondreduced-pressure interface coupled to the over-drape, wherein the secondreduced-pressure interface is sized and configured to receive asubcutaneous delivery conduit and to form a fluid seal between thesubcutaneous delivery conduit and the wound dressing assembly. Themethod further includes fluidly coupling a reduced-pressure deliveryconduit to a reduced-pressure source and the first reduced-pressureinterface, delivering reduced pressure to the reduced-pressure deliveryconduit, fluidly coupling a subcutaneous delivery conduit to the secondinterface, and delivering reduced pressure to the subcutaneous deliveryconduit.

According to another illustrative embodiment, a method of manufacturinga wound dressing assembly for treating damaged subcutaneous damagedtissue includes providing a dressing bolster formed from a medicalbolster material. The dressing bolster is for placing on a patient'sepidermis and is substantially sized to overlay a linear wound. Themethod further includes providing an over-drape for providing a fluidseal over the dressing bolster and a portion of the patient's epidermis,providing a reduced-pressure source, providing a first reduced-pressureinterface for delivering reduced pressure to the dressing bolster,providing a second reduced-pressure interface, and coupling the secondreduced-pressure interface to the over-drape, wherein the secondreduced-pressure interface is sized and configured to receive asubcutaneous delivery conduit and to form a fluid seal therebetween.

Other features and advantages of the illustrative embodiments willbecome apparent with reference to the drawings and the detaileddescription that follow.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic perspective view, with a portion shown incross-section, of an illustrative reduced-pressure system for treating atissue site having a linear wound that includes a first reduced-pressureinterface and a second reduced-pressure interface;

FIG. 2 is a schematic, cross-sectional view of the illustrativereduced-pressure system of FIG. 1;

FIG. 3A is a schematic, perspective view of a portion of an illustrativedressing bolster that forms a part of a reduced-pressure system;

FIG. 3B is a schematic, perspective view of a portion of an illustrativedressing bolster that forms a part of a reduced-pressure system;

FIG. 4 is a schematic, perspective view of a portion of a wound dressingassembly for treating a tissue site having a linear wound;

FIG. 5 is a schematic, perspective view of a portion of a wound dressingassembly for treating a tissue site having a linear wound;

FIG. 6 is a partially-exploded, schematic perspective view, with aportion in cross-section, of an illustrative embodiment of a wounddressing assembly having a second reduced-pressure interface;

FIG. 6A is a detail of a portion of the wound dressing assembly of FIG.6;

FIG. 7 is a schematic, side cross-sectional view of an illustrativereduced-pressure system for treating a tissue site having a linear woundand providing a subcutaneous delivery conduit to a subcutaneous tissuesite;

FIG. 8 is a schematic, exploded, perspective view of an illustrativeembodiment of a wound dressing assembly that includes a secondreduced-pressure interface; and

FIG. 9 is a schematic, perspective view of an illustrative embodiment ofa wound dressing assembly having a first reduced-pressure interface anda second reduced-pressure interface.

DETAILED DESCRIPTION OF ILLUSTRATIVE EMBODIMENTS

In the following detailed description of the illustrative embodiments,reference is made to the accompanying drawings that form a part hereof.These embodiments are described in sufficient detail to enable thoseskilled in the art to practice the invention, and it is understood thatother embodiments may be utilized and that logical structural,mechanical, electrical, and chemical changes may be made withoutdeparting from the spirit or scope of the invention. To avoid detail notnecessary to enable those skilled in the art to practice the embodimentsdescribed herein, the description may omit certain information known tothose skilled in the art. The following detailed description is,therefore, not to be taken in a limiting sense, and the scope of theillustrative embodiments are defined only by the appended claims.

As a result of a surgery or other medical condition, a patient may havea subcutaneous wound that is located near or beneath a linear wound onthe patient's epidermis. For example, after a surgery to removesubcutaneous tissue from a patient, the patient may have a linear woundas a result of the surgical incision. The patient may also have an areabeneath their skin that will need to heal as a result of the surgery,i.e., a subcutaneous wound or defect.

In such a case, the subcutaneous wound may exude or collect fluidsduring the healing process, and a drain may be inserted at or near theend of the linear wound in order to collect exudates and prevent thecollection of unwanted fluids at the tissue site of the subcutaneouswound. The drain may be connected to a drain tube, which may be referredto as a subcutaneous delivery conduit, that is configured to exit thepatient's body at one end of the linear wound. The drain tube, which isa type of subcutaneous delivery conduit, may be connected to a drain forthe purposes of collecting wound exudates in a sanitary fashion.Contemporaneously, a reduced-pressure treatment method may be applied totreat the linear wound that was caused during the surgery. Thereduced-pressure treatment method involves the formation of a fluid sealover the treatment area that includes the linear wound.

The fluid seal is typically an important and fragile feature of a systemthat delivers reduced pressure to a wound site. Any breach in the fluidseal may cause a leak that may shut down or otherwise compromise areduced-pressure delivery system because such systems tend to be highlyintolerant of leaks. One method for providing the fluid seal may be toprovide a wound dressing assembly that includes a pliable drape, orover-drape, that seals against the epidermis of the patient. By formingthe fluid seal, the over-drape may preserve a pressure differentialbetween the treatment area and the ambient environment, which may alsobe referred to as the external environment. As used throughout thisdocument, the term “or” does not require mutual exclusivity. In caseswhere a drain tube is present, application of a reduced-pressure wounddressing assembly may be difficult because the drain tube may preventthe over-drape from sealing against the patient's epidermis. In caseswhere a treatment provider attempts to seal the treatment area byapplying the over-drape over the drain tube, a leak may result. Further,even if a fluid seal can be obtained, movement of the drain tube mayentirely disrupt the seal and cause a loss of reduced pressure at thetreatment site, thereby compromising the ability to maintain the desiredamount of reduced pressure at the tissue site. Thus, it is desirable tohave a dressing assembly or interface for allowing a drain tube, orsubcutaneous delivery conduit, to pass through a reduced-pressuretreatment area (from a drain to a drain collection area) withoutdisrupting the fluid seal between the treatment site and the ambientenvironment.

Referring now primarily to FIG. 1, an illustrative embodiment of areduced-pressure treatment system 110 for treating a tissue site 112that includes a linear wound 114, while simultaneously collecting woundexudates through a drain 136, is presented. The tissue site 112 isrelated to a linear wound 114. The tissue site 112 may be the bodilytissue of any human, animal, or other organism, including bone tissue,adipose tissue, muscle tissue, dermal tissue, vascular tissue,connective tissue, cartilage, tendons, ligaments, or any other tissue.Treatment of the tissue site 112 may include removal of fluids, e.g.,exudate. The tissue site 112 is shown at epidermis 116, but in somecases may also involve the dermis 118, and subcutaneous tissue 120. Thereduced-pressure treatment system 110 may also be used with other tissuesites.

The reduced-pressure treatment system 110 includes a wound dressingassembly 122 and a reduced-pressure subsystem 111. While thereduced-pressure treatment system 110 is shown in the context of areduced-pressure wound dressing assembly 122 placed over a linear wound114, it should be understood that the reduced-pressure treatment system110 may be used on other tissue sites, including open wounds. The wounddressing assembly 122 includes a dressing bolster 124 that functions asa manifold, an over-drape 126, and a first reduced-pressure interface128 to accommodate a reduced-pressure delivery conduit 130. Thereduced-pressure delivery conduit 130 is fluidly coupled to thereduced-pressure subsystem 111.

Functionally, the reduced pressure developed by the reduced-pressuresubsystem 111 is delivered through the reduced-pressure delivery conduit130 to the first reduced-pressure interface 128. In one illustrativeembodiment, the first reduced-pressure interface 128 is a T.R.A.C.® Pador Sensa T.R.A.C.® Pad available from KCI of San Antonio, Tex. The firstreduced-pressure interface 128 allows the reduced pressure to bedelivered to the dressing bolster 124. In another embodiment, noreduced-pressure interface 128 is used. Instead, a lumen (or conduit) isplaced through the over-drape 126 directly into the dressing bolster124.

The wound dressing assembly 122 provides a fluid seal over an area thatincludes a tissue site 112 that is to be treated with reduced pressure.A fluid seal is a seal adequate to maintain reduced pressure at adesired site given the particular reduced-pressure source(s) orsubsystem involved.

The wound dressing assembly 122 also includes a second reduced-pressureinterface 132. The second reduced-pressure interface 132 is fastened tothe over-drape 126 by an adhesive, bond, weld (e.g., an ultrasonic,thermal, or RF weld), or cement (not shown). The second reduced-pressureinterface 132 maintains the integrity of the fluid seal over the tissuesite 112 while allowing a subcutaneous delivery conduit 134 to passthrough the dressing bolster 124 and over-drape 126. In an embodiment,the second reduced-pressure interface 132 comprises a molded plasticcomponent that is welded or adhered to the over-drape 126.

The second reduced-pressure interface 132 of FIG. 1 is configured sothat a user or treatment provider can exert a force against an outersurface of the second reduced-pressure interface 132 to route asubcutaneous delivery conduit 134 through the wound dressing assembly122. At the same time, the user can press a subcutaneous deliveryconduit 134 against the over-drape 126 at the location of the secondreduced-pressure interface 132 with sufficient force to breach theover-drape 126. The second reduced-pressure interface 132 reinforces theover-drape 126 so that it can be breached without compromising theability of the over-drape 126 to provide a fluid seal outside of thesecond reduced-pressure interface 132. In one embodiment, an aperture isformed in the over-drape at the second reduced-pressure interface 132 tofacilitate a pathway through the wound dressing assembly 122.

The second reduced-pressure interface 132 may take any number of shapesand sizes. For example, the second reduced-pressure interface 132 may beshaped substantially as shown in FIG. 1, where the secondreduced-pressure interface 132 includes flat top and bottom surfaces andan aperture 168. The aperture 168 may be sized to generate a radialcompressive force against a subcutaneous delivery conduit 134 when thesubcutaneous delivery conduit 134 is inserted through the secondreduced-pressure interface 132. For example, an interference fit may beformed between the aperture 168 and the subcutaneous delivery conduit134. According to one illustrative embodiment, the secondreduced-pressure interface 132 may comprise a nipple 131 formed from aninterface body 133 with the aperture 168 having an interior diameter D₁.The subcutaneous delivery conduit 134 may have an external diameter D₂.The diameters are related by the expression D₁<D₂. D₁ is slightly lessthan D₂ whereby the fluid seal is formed by an interference fit. Inanother embodiment, D₁ may be equal to D₂.

The second reduced-pressure interface 132 may also be tapered such thatthe thickness of the second reduced-pressure interface 132 is increasedat the aperture and gradually decreased to a minimal thickness at theouter edge. The thickness of the second reduced-pressure interface 132may gradually increase from the edge to the boundary of the aperture 168in a linear or curved manner. The second reduced-pressure interface 132may also have a rounded, or dome-typed shape. Other shapes are possibleas well.

The subcutaneous delivery conduit 134 functions to allow wound exudatesto flow from a subcutaneous tissue site 138 from a drain 136. Thesubcutaneous delivery conduit 134 may fluidly couple to thereduced-pressure subsystem 111 or a second reduced-pressure subsystem(not shown). Thus, both the reduced-pressure delivery conduit 130 andsubcutaneous delivery conduit 134 provide reduced pressure and maycouple to the reduced-pressure subsystem 111. Here, the reduced-pressuredelivery conduit 130 is coupled to the reduced-pressure subsystem 111 toapply reduced-pressure therapy to a tissue site 112. The subcutaneousdelivery conduit 134 may also couple to the reduced-pressure subsystem111, or to a separate reduced-pressure subsystem (not shown) to evacuatefluids, or exudates, from a drain 136.

Reduced pressure is a pressure less than the ambient pressure at atissue site that is being subjected to treatment. In most cases, thisreduced pressure will be less than the atmospheric pressure at which thepatient is located. Alternatively, the reduced pressure may be less thana hydrostatic pressure at the tissue site. Unless otherwise indicated,values of pressure stated herein are gauge pressures. The reducedpressure delivered may be constant or varied (patterned or random) andmay be delivered continuously or intermittently. Consistent with the useherein, unless otherwise indicated, an increase in reduced pressure orvacuum pressure typically refers to a relative reduction in absolutepressure.

In some embodiments, a different amount of reduced pressure may bedesired at the tissue site 112 of the linear wound 114 than at thesubcutaneous tissue site 138. In such embodiments, the subcutaneousdelivery conduit 134 and reduced-pressure delivery conduit 130 may befluidly coupled to different reduced-pressure sources and may includedifferent fluid reservoirs associated with each. Alternatively, thedelivery conduits 130, 134 may be coupled to the same reduced-pressuresubsystem 111 through one or more pressure regulators 140 that allow asingle reduced-pressure subsystem 111 to supply different amounts ofreduced pressure to each conduit. In some embodiments, the same amountof reduced pressure may be desired at the tissue site 112 of the linearwound 114 as the subcutaneous tissue site 138. In these embodiments, thesubcutaneous delivery conduit 134 and reduced-pressure delivery conduit130 may be fluidly coupled to the same reduced-pressure source 109without the need for pressure regulators.

Referring now primarily to FIG. 2, a side cross section of the wounddressing assembly 122 of FIG. 1 is presented. The wound dressingassembly 122 as shown includes an optional inner comfort layer 142 thatmay be coupled to the dressing bolster 124 and that lies between thedressing bolster 124 material and the epidermis 116 of a patient. Thewound dressing assembly 122 may also include (latitudinal orlongitudinal) flexibility notches 144 in order to add flexibility to thedressing bolster 124. Additionally, the over-drape 126 of wound dressingassembly 122 may include folds 146 or notches or ridges to addflexibility to the wound dressing assembly 122.

In addition to the first reduced-pressure interface 128 that is fluidlycoupled to the reduced-pressure delivery conduit 130 and dressingbolster 124, the wound dressing assembly 122 also includes the secondreduced-pressure interface 132. The second reduced-pressure interface132 functions to accommodate the presence of a subcutaneous deliveryconduit 134. The subcutaneous delivery conduit 134 functions as a draintube that is fluidly coupled to a drain 136 without disturbing theability of the reduced-pressure treatment system 110 to apply reducedpressure to a tissue site 112. The second reduced-pressure interface 132fluidly couples a reduced pressure source to the drain 136 withoutcausing a leak that hinders or stops the reduced-pressure therapy attissue site 112.

The dressing bolster 124 of the wound dressing assembly 122 has a firstside 148 and a second, inward-facing side 150. The dressing bolster 124may be formed from any bolster material or manifold material thatprovides a vacuum space, or treatment space, such as a porous andpermeable foam or foam-like material, a member formed with pathways, agraft, or gauze. As a more specific, non-limiting example, the dressingbolster 124 may be a reticulated, open-cell polyurethane or polyetherfoam that allows good permeability of wound fluids while under a reducedpressure. One such foam material that has been used is a VAC® GranuFoam®material available from Kinetic Concepts, Inc. (KCI) of San Antonio,Tex. Any material or combination of materials may be used for themanifold material provided that the manifold material is operable todistribute the reduced pressure.

A manifold is generally a substance or structure that is provided toassist in applying reduced pressure to, delivering fluids to, orremoving fluids from a tissue site. A manifold typically includes aplurality of flow channels or pathways. The plurality of flow channelsmay be interconnected to improve distribution of fluids provided to andremoved from the area of tissue around the manifold. Examples ofmanifolds may include, without limitation, devices that have structuralelements arranged to form flow channels, cellular foam, such asopen-cell foam, porous tissue collections, and liquids, gels, and foamsthat include or cure to include flow channels. In some embodiment, themanifold may be formed by a plurality of layers or substrates. Moreover,in some embodiments of the manifold with multiple layers, the layer thatis closest to the patient during use may be the least hydrophilic andthe most hydrophobic material.

The reticulated pores of the GranuFoam® material are helpful in carryingout the manifold function, but again other materials may be used. Amaterial with a higher, or lower, density (smaller pore size) thanGranuFoam® material may be desirable in some situations. Among the manypossible materials, the following may be used: GranuFoam® material,Foamex® technical foam (www.foamex.com), gauze, a flexiblechannel-containing member, a graft, etc. In some instances it may bedesirable to add ionic silver to the foam in a micro-bonding process orto add other substances to the material, such as antimicrobial agents.

The manifold typically includes a plurality of flow channels or pathwaysthat distribute fluids provided to and removed from the tissue sitearound the manifold. Here, the manifold may be a biocompatible materialthat is capable of being placed in contact with the subcutaneous tissuesite and distributing reduced pressure to the subcutaneous tissue site.The manifold material may include a bioresorbable material that mayremain in a patient's body following the reduced-pressure treatment.Generally, the bioresorbable material is a material that enzymaticallyor chemically degrades into a simple chemical species in vivo, and whichmay be removed from the body by excretion of metabolism. Suitablebioresorbable materials may include, without limitation, a polymericblend of polylactic acid (PLA) and polyglycolic acid (PGA). Thepolymeric blend may also include without limitation polycarbonates,polyfumarates, and capralactones. The manifold material may furtherserve as a scaffold for new cell-growth, or a scaffold material may beused in conjunction with the manifold material to promote cell-growth. Ascaffold is a substance or structure used to enhance or promote thegrowth of cells or formation of tissue, such as a three-dimensionalporous structure that provides a template for cell growth. Illustrativeexamples of scaffold materials include calcium phosphate, collagen,PLA/PGA, coral hydroxy apatites, carbonates, or processed allograftmaterials.

In one illustrative embodiment, the dressing bolster 124 is manufacturedas follows. A foam block of Granufoam® material, e.g., 1.21 meter×1.8meter×0.5 meter block, is cut to have a 19 mm height, and a saw is usedto form lateral grooves, or lateral flexibility notches as shown inFIGS. 2 and 6. Then, a dry layer, which may be the inner comfort layer142, is laminated or attached onto the second, or bottom, surface. Thefoam block is then cut using a die cut to form individual dressingbolsters 124.

The optional inner comfort layer 142 has a first side 152 and a second,inward-facing side 154. The first side 152 of the optional inner comfortlayer 142 may be coupled, for example, by a heat bond or any othertechnique, to the second, inward-facing side 150 of the dressing bolster124. The inner comfort layer 142 typically provides for patient comfortwhen the dressing bolster 124 is placed adjacent to the patient'sepidermis 116. The inner comfort layer 142 may be any material thathelps prevent skin irritation and discomfort while allowing fluidtransmission through the inner comfort layer 142. As non-limitingexamples, a woven, elastic material or a polyester knit textilesubstrate may be used. As another non-limiting example, an InterDry™textile material from Milliken Chemical, a division of Milliken &Company, Inc. of Spartanburg, S.C., may be used. The inner comfort layer142 may include anti-microbial substances, such as silver, and may bemade like a breathable, dry layer.

The dressing bolster 124 may include a plurality of flexibility notches144 or recesses that may be lateral cuts in the dressing bolster 124 onthe first side 148. In addition, the flexibility notches 144 may be oneor more longitudinal notches, or longitudinal cuts, or other cuts. Thecuts may be made using a saw (or notched blade), a hot knife, or otherdevice. The flexibility notches enhance flexibility of the dressingbolster 124. The enhanced flexibility may be particularly useful whenthe wound dressing assembly 122 is applied over a patient's joint areaor another area of movement. For example, if the dressing bolster 124 isused on a knee, the dressing bolster 124 may need to flex or extend asmuch as 100% or more and the flexibility notches help provide thedesired flexibility. The flexibility notches may also take variousshapes, such as hexagons, slits, or squares.

The dressing bolster 124 may be formed with lateral edges that areorthogonal with respect to the second, inward-facing side 150 of thedressing bolster 124. The lateral edges may also be formed with abeveled edge or angled edge. The angled or beveled edge may distributeshear stress between the dressing bolster and the patient's epidermis116. The dressing bolster 124 may also have rounded sides. The dressingbolster 124 may have a small aperture, or cut, formed through thebolster to lead the subcutaneous delivery conduit 134 through thedressing bolster 124 with relatively less force.

A sealing member, which is shown as the over-drape 126, provides a fluidseal over the dressing bolster 124 and at least a portion of thepatient's epidermis 116. As such, the over-drape 126 may be formed fromany material that allows for a fluid seal. The over-drape 126 may besealed against epidermis 116 or against a gasket material by a sealingapparatus, such as a pressure-sensitive adhesive.

The sealing apparatus may take numerous forms, such as an adhesivesealing tape, or drape tape or strip; double-side drape tape;pressure-sensitive adhesive; paste; hydrocolloid; hydrogel; or othersealing means. As discussed herein, the sealing member is commonly anover-drape 126. If a tape is used, the tape may be formed of the samematerial as the over-drape 126 with a pre-applied, pressure-sensitiveadhesive. The pressure-sensitive adhesive may be applied on a second,inward-facing side 158 of the over-drape 126 or portion thereof. Thepressure-sensitive adhesive helps provide a fluid seal between theover-drape 126 and the epidermis 116. As used herein, the fluid seal mayalso include a gasket against the epidermis 116. Before the sealingmember is secured to the epidermis, removable strips, or release liners,covering the pressure-sensitive adhesive may be removed.

The sealing member, or over-drape 126, may be an elastomeric material orany material or substance that provides a fluid seal. Examples ofelastomers may include, but are not limited to, natural rubbers,polyisoprene, styrene butadiene rubber, chloroprene rubber,polybutadiene, nitrile rubber, butyl rubber, ethylene propylene rubber,ethylene propylene diene monomer, chlorosulfonated polyethylene,polysulfide rubber, polyurethane, EVA film, co-polyester, and silicones.Further still, sealing member materials may include a silicone drape, 3MTegaderm® drape, acrylic drape such as one available from AveryDennison, or an incise drape.

The sealing member, or over-drape 126, may include a first sealingmember or drape portion 160 and a second sealing member or drape portion162. The first sealing drape portion 160 extends over the first side 148of the dressing bolster 124. The over-drape 126 extends further to forma sealing member flange, or sealing member extension, which has a firstside and a second, inward-facing side (not explicitly shown). Anaperture (not explicitly shown but analogous to 559 in FIG. 8) is formedon a portion of the over-drape 126 to allow fluid communication with afirst reduced-pressure interface 128, which is fluidly coupled to thereduced-pressure subsystem 111.

The second, inward-facing side of the over-drape extension is placed ona first side (top side for the orientation of FIG. 1) of the secondsealing drape portion 162 and coupled, such as by an adhesive, bond,welding (e.g., ultrasonic, thermal or RF welding), or cements (notshown). Alternatively, the first sealing drape portion 160 and secondsealing drape portion 162 may be integrally formed. The first sealingdrape portion 160 may include a plurality of folds 146, or stretchzones. The folds 146 allow additional drape material to becomeavailable, to stretch, or to move, if needed. For example, if the wounddressing assembly 122 is used on a joint, when the joint is flexed,additional drape material may be to useful accommodate movement of thejoint. The folds 146 facilitate such movement.

Prior to application, one or more release members (not shown butanalogous to 581 and 583 in FIG. 8) may be releasably coupled to thefirst side of the second sealing drape portion 162. The release membersprovide stiffness and help during deployment of the wound dressingassembly 122. The release members are typically either casting paper ora film held on the first side of the second sealing drape portion 162.

The reduced-pressure subsystem 111 includes at least onereduced-pressure source 109, which can take many different forms. Thereduced-pressure source 109 provides reduced pressure as a part of thereduced-pressure treatment system 110. The reduced-pressure source 109is fluidly coupled to the first reduced-pressure interface 128 by thereduced-pressure delivery conduit 130.

The reduced-pressure subsystem 111 may have one or more of a reservoirregions 113 or canister regions. The reservoir region 113 or canisterregion may include one or more filters to protect the pneumatic systemfrom the ingress of liquids from the tissue site 112 or subcutaneoustissue site 138. An interposed membrane filter, such as a hydrophobic oroleophobic filter, may be interspersed between the reduced-pressuredelivery conduit 130 and the reduced-pressure subsystem 111. One or moredevices may be fluidly coupled to the reduced-pressure delivery conduit130 in addition to the reduced-pressure subsystem 111. For example,another fluid reservoir or collection member to hold exudates and otherfluids removed, a pressure-feedback device, a volume detection system, ablood detection system, an infection detection system, a flow monitoringsystem, or a temperature monitoring system may be coupled to thereduced-pressure delivery conduit 130. Such devices may be included inor formed integrally to the reduced-pressure subsystem 111.

The reduced-pressure subsystem 111 may be any device for supplying areduced pressure, such as a vacuum pump, wall suction, or other source.While the amount and nature of reduced pressure applied to a tissue sitewill typically vary according to the application, the reduced pressurewill typically be between −5 mm Hg (−667 Pa) and −500 mm Hg (−66.7 kPa)and more typically between −75 mm Hg (−9.9 kPa) and −300 mm Hg (−39.9kPa). For example, and not by way of limitation, the pressure may be−12, −12.5, −13, −14, −14.5, −15, −15.5, −16, −16.5, −17, −17.5, −18,−18.5, −19, −19.5, −20, −20.5, −21, −21.5, −22, −22.5, −23, −23.5, −24,−24.5, −25, −25.5, −26, −26.5 kPa or another pressure.

The reduced pressure developed by reduced-pressure subsystem 111 isdelivered through the reduced-pressure delivery conduit 130 to the firstreduced-pressure interface 128. The first reduced-pressure interface 128allows the reduced pressure to be delivered through the over-drape 126to the dressing bolster 124.

In providing treatment with the reduced-pressure treatment system 110,it may be desirable to know that reduced pressure of at least a certainthreshold level is being delivered to the tissue site 112. A dressingreduced-pressure indicator coupled to the reduced-pressure source canaccomplish this task. The dressing reduced-pressure indicator may alsobe a separate unit fluidly coupled to the over-drape 126 such thatpressure from within the sealed space of the over-drape 126 reaches thedressing reduced-pressure indicator or may be associated with the firstreduced-pressure interface 128 as part of the reduced-pressure subsystem111. When adequate reduced pressure is present, the reduced-pressureindicator may assume a collapsed position and when inadequate reducedpressure is present the reduced-pressure indicator may assume anon-collapsed position.

In some embodiments, the dressing bolster 124 is pre-formed toaccommodate the presence of a subcutaneous delivery conduit 134 that mayor may not be present. As shown in FIG. 3A, a dressing bolster 224 maybe pre-formed to optionally receive a subcutaneous delivery conduit bythe formation of a relieved area such as a perforated cut 264 orperforated cylinder of bolster material. To allow for easy passage ofthe conduit through the dressing bolster, the perforated cylinder ofbolster material can be removed or punched out of the dressing bolster224 by hand when a drain is to be applied. Additionally, it may bedesirable to perforate the bolster material with multiple cuts ofvarious diameters so that a piece of bolster material that isapproximately the size of any foreseeable drain tube size can be removedby hand.

Alternatively, where slightly more deformation in the dressing bolster224 is tolerable, the dressing bolster 224 may have a relieved area inthe form of a cross-cut 266 made in the bolster material as shown inFIG. 3B to allow for the passage of a drain tube. The perforated cut 264may be any variety of perforated shapes or sizes depending on the typeof conduit or tubing to be routed through the dressing bolster 224. Incases where the dressing bolster 224 is assembled with an optionalcomfort layer, such as inner comfort layer 142 of FIG. 2, theperforation or cross-cut may also be formed in the inner comfort layer142 to complement the perforated cut 264 or cross-cut 266 in thedressing bolster material.

Referring now primarily to FIG. 4 a wound dressing assembly 222 thatincorporates a dressing bolster 224 having a relieved area is shown. Thewound dressing assembly 222 components may have a perforated cut 264 orcross-cut 266 (FIG. 3B) to allow for the easy removal of a cylinder ofdressing bolster material in order for a subcutaneous delivery conduitto pass through the dressing bolster 224. In such embodiments, theperforated cut 264 or cross-cut 266 may extend through only part of thewound dressing assembly so that a fluid seal is maintained at a tissuesite whether or not a subcutaneous delivery conduit is present. Thewound dressing assembly includes a second reduced-pressure interface 232to form a fluid seal at the boundary of the second reduced-pressureinterface 232 and subcutaneous delivery conduit if one is present. Thesecond reduced-pressure interface 232 may function to reinforce the sealprovided by the over-drape 226 between a tissue site and the ambientenvironment. Here, the second reduced-pressure interface 232 alsoincludes an aperture 268 for allowing a section of conduit to be routedthrough the second reduced-pressure interface 232.

Referring now primarily to FIG. 5, the second reduced-pressure interface232 may be molded using a material with elastomeric properties, i.e., anelastomer, as discussed above. The elasticity of the material of thesecond reduced-pressure interface 232 enables the aperture 268 in thesecond reduced-pressure interface 232 to expand to allow a section ofconduit, or subcutaneous delivery conduit 234 to pass through theaperture 268. In one embodiment, the aperture 268 may be of a slightlysmaller diameter than the diameter of the conduit that may route throughthe second reduced-pressure interface 232. This slight overlap in sizingmay achieve an interference fit that causes the aperture 268 to undergoa small amount of deformation when a subcutaneous delivery conduit 234is routed through the second reduced-pressure interface 232.

As a result of the deformation, elastomeric properties (i.e.,elasticity) of the second reduced-pressure interface 232 may generate aradial compressive force 270 between the surface of the aperture 268 andthe subcutaneous delivery conduit 234. The radial compressive force 270may thereby form a fluid seal at the boundary of the secondreduced-pressure interface 232 and subcutaneous delivery conduit 234,thereby preserving the pressure differential between the tissue site andthe ambient environment. In some cases, additional materials may be usedto form or strengthen this sealed boundary of the secondreduced-pressure interface 232 and the subcutaneous delivery conduit234. For example, adhesives or one or more gaskets (for example, ano-ring) may be installed between the surface of the aperture 268 and theouter surface of the subcutaneous delivery conduit 234 to enhance thestrength of the fluid seal.

Referring now primarily to FIG. 6, another embodiment of areduced-pressure system 300 for treating a tissue site having a linearwound (not shown) is presented. The reduced pressure system 300 includessecond reduced-pressure interface 332 that is incorporated into a wounddressing assembly 322 to be applied to a tissue site (not shown). Thetissue site is proximate to a first conduit segment 335 of thesubcutaneous delivery conduit 334. In some cases, it may be desirable toallow the first conduit segment 335 of subcutaneous delivery conduit 334to remain installed in subcutaneous tissue 320 and to apply a wounddressing assembly 322 over the inserted conduit while disturbing thesurrounding tissue as little as possible. Here, a more modular solutionis shown for applying a wound dressing assembly 322 to deliver reducedpressure to a linear wound (not shown) that is located near the point inthe patient's epidermis where the subcutaneous delivery conduit 334exits the patient's epidermis or skin.

The subcutaneous delivery conduit 334 may include a first conduitsegment 335 that extends only a small distance (e.g., about 10centimeters) above a patient's epidermis 316 and that is subsequentlycoupled to additional sections of conduit, e.g., second segment 376 oradapter 397. The combined conduit segments 335, 397, and 376 (or in someembodiments, 335 and 376) are used to evacuate collected fluids. Thefirst conduit segment 335 of the subcutaneous delivery conduit 334 mayremain installed in the patient and be sized, trimmed, or otherwiseconfigured to protrude from the epidermis 316 enough to allow a sealedcoupling between an end portion 396 of the first conduit segment 335 andan end portion 374 of a second conduit segment 376. The second conduitsegment 376 may be fluidly coupled to a reduced-pressure source anddrainage collection area (not shown). The second conduit segment 376 ofthe subcutaneous delivery conduit 334 may be removed and replacedwithout removing the first conduit segment 335.

The coupling between the first conduit segment 334 and second conduitsegment 376 may occur in a number of ways. For example, an effectivecoupling may be achieved by providing an interference fit between theend portion 335 of the first conduit segment 334 to the second conduitsegment 376. This coupling may be a direct coupling or a coupling madeusing the adapter 397, or coupler, that includes an intermediate conduitsegment. If an adapter 397 is not used, the first conduit segment may besized to protrude through the wound dressing assembly 322 and the secondreduced-pressure interface 332, and the end portion (or distal end) 374of the second conduit segment 376 may be sized to fit snugly over theend portion 396 of the first conduit segment 335. The overlap of conduitsegments (335 and 376) forms a liquid-tight seal.

The adapter 397 may be a coupler having tapered conduit ends adapted toform fluid seals with both the first conduit segment 335 and secondconduit segment 376. Any sealing means used to couple the adapter 397 tothe first conduit segment 335 and second conduit segment 376 mayalternatively be used to couple the first conduit segment 335 directlyto the second conduit segment 376. For example, overlapping portions ofthe first conduit segment 335 and second conduit segment 376 may beforced together to form the coupling. Additionally, the second conduitsegment 376 may receive a grooved conduit segment 380 on the end segment378 of the adapter 397, as suggested in FIG. 6A, or a grooved segment ofthe first conduit segment 335. The end portions of the conduit segmentsmay also include other physical features to aid in forming andpreserving a seal. For example, the outer surface of a smaller conduitportion may be angled, or tapered and the inner surface of a largerdiameter conduit portion may have complementary grooves or a taper toreceive and seal against the opposing conduit segment.

A securing member 384 may be optionally included to secure the firstconduit segment 335 relative to the epidermis 316 to minimize irritationof the surrounding tissue during the application of the dressingassembly 322. As such, a securing member 384 may be of a low hardnessmaterial that is very flexible and transmissive to moisture tosubstantially eliminate or reduce irritation and damage to theunderlying dermis. The securing member 384 material may be porousmaterial, such as a sintered rubber or silicone polymer member. Asecuring member 384 may adhere to the epidermis 316 using an adhesive orother attachment device. The securing member 384 helps secure the firstconduit segment 335 in order to prevent unwanted movement of the firstconduit segment 335. The securing member 384 may take the shape of aring, or may have a flanged shape as shown in FIG. 6. In such anarrangement, the securing member 384 may function as an intermediateconduit segment and form a sealed coupling between the first conduitsegment 334 and second conduit segment 376 or may be a pass throughdevice that only secures the conduit segments 335 and 376.

Referring now primarily to FIG. 7, another reduced-pressure system 400for treating a tissue site having a linear wound is presented thatincludes a second reduced-pressure interface 432. A wound dressingassembly 422 is analogous to the wound dressing assembly 122 of FIG. 2in many respects. However, the over-drape 426 is more loose fitting andcan be formed over the second reduced-pressure interface 432 and securedagainst the subcutaneous delivery conduit 434 with an o-ring 486 orclamp. The second reduced-pressure interface 432 may include a nipple431 formed from an interface body 433.

Referring now primarily to FIG. 8, an exploded perspective view of aportion of a wound dressing assembly 522 for application in treating atissue site with reduced pressure is presented. The tissue site may be asubcutaneous tissue site, a linear wound, area wound, or other wound orgraft. The wound dressing assembly 522 presented in FIG. 8 is shown in apre-deployment state and in an exploded view. The wound dressingassembly 522 is analogous in most respects to the wound dressingassembly 122 and of FIGS. 1 and 2. To indicate corresponding parts, thereference numerals have been indexed by 100 and may not be furthermentioned.

The wound dressing assembly 522 includes a dressing bolster 524, whichin turn may include flexibility notches 544 in both the lateral andlongitudinal directions relative to the surface of the dressing bolster524. The first side 548 of the dressing bolster 524 is covered by anover-drape 526, which may include a first drape portion 560 and a seconddrape portion 562. The first drape portion 560 includes folds 546 and adrape aperture 559. The second drape portion 562 is formed with atreatment area aperture 588 that provides an opening for at least aportion of the dressing bolster 524 or an inner comfort layer 542 to beapplied directly against a patient's epidermis. The second drape portion562 has first side 587 and has an adhesive 589 applied on a portion ofthe first side 587. The adhesive 589 is used primarily duringmanufacture to hold the dressing bolster 524 (or inner comfort layer 542if present) against the second drape portion 562 during assembly andalso used to help hold the dressing bolster 524 during use. Beforeapplying the dressing bolster 524 or inner comfort layer 542 against theadhesive 589, the adhesive 589 is covered by a center releasable member585. Outboard of the adhesive 589 on the first side 587 are releasablemembers 583 that provide stiffness to the over-drape 526 duringdeployment.

The second, inward-facing side (not explicitly shown but opposite sideof the first side 587) of the second drape portion 562 may be coveredwith an adhesive. In the pre-deployment state, this adhesive is coveredby a bottom release member 590 and side release members 583.

Once assembled, the wound dressing assembly 522 may resemble thedressing assembly 122 of FIG. 1. The use and design may vary, but in oneillustrative embodiment, the wound dressing assembly 522 may deployed asdescribed below. A subcutaneous delivery conduit (not shown) may beinserted into the patient and then a distal end placed through the wounddressing assembly 522 from a second side to the first side. In oneembodiment, the subcutaneous delivery conduit is pushed throughpreformed cuts 566 in the comfort layer 542 (if present) and optionallythrough the dressing bolster 524.

The bottom release liner 590 is removed and exposed adhesive on thesecond, inward-facing side of the second drape portion 562 is placedagainst a portion of the patient's epidermis beginning at one end andthe wound dressing assembly 522 may be placed over a linear wound. Aftersmoothly applying the second drape portion 562, the side release members583 are removed. The release members 581 on the first side 587 of theover-drape 526 are removed. A first reduced-pressure interface 528 iscoupled to the drape aperture 559 in the first drape portion 560. Asecond reduced-pressure interface 532 may also be adhered to the drape(if not already applied during manufacture) at a location that iscoaxial with the center of pre-formed cuts 566 made in the dressingbolster 524 and inner comfort layer 542 (if present) to accommodate thepresence of a drain. The center release member 585 would have beenremoved during manufacture.

A user or treatment provider may apply the wound dressing assembly 522,that includes the second reduced-pressure interface 532 with the drainor other subcutaneous delivery tube within the footprint of the wounddressing assembly 522. In one embodiment, the second reduced-pressureinterface is installed in the wound dressing assembly duringmanufacture. In another embodiment, the second reduced-pressureinterface 532 is a separate item that may be added at the time of use.For example, a drain tube may protrude from the end of a surgical woundand therefore a user would recognize that the second reduced-pressureinterface 532 is desired and apply the second reduced-pressure interface532.

In the application of one embodiment, after selecting the wound dressingassembly, the user would orient the wound dressing assembly 522 suchthat pre-formed cuts 566 in the dressing bolster are aligned with thesubcutaneous delivery conduit of the drain. The user would then pressthe conduit through the dressing bolster until the user felt theresistance of the over-drape 526. The user would apply a force to themolded reduced-pressure interface to push the conduit through the drape,which breaches when subjected to a critical force. In order to apply thecritical force, the reduced-pressure interface may need to be of anadequate size for a user to grip the material that forms the interfaceand press it against the conduit. For example, the secondreduced-pressure interface may need to extend for at least onecentimeter radially past the aperture through which the conduit passes.The user would then draw a sufficient amount of conduit through thewound dressing assembly 522 to allow for the placement of the wounddressing assembly 522 before connecting the conduit to a receptacle.This method of application should result in both the secondreduced-pressure interface and the breached over-drape exerting radialcompression about the conduit to form a fluid seal at the border of theconduit and wound dressing assembly 522.

In a similar embodiment, the second reduced-pressure interface 532 maybe added at the time of deployment. In cases where a subcutaneousdelivery conduit is present near the wound site, the conduit may berouted through pre-formed cuts 566, or through similar newly formedcuts. Similarly, a distal end of the conduit may be pressed through aportion of the over-drape 526 that is designed to be punctured orthrough a newly formed incision in the drape. The secondreduced-pressure interface 532 may be placed over the distal end of thesubcutaneous delivery conduit, slid over the subcutaneous deliveryconduit, and adhered to the outer surface of the over-drape 526. Thedistal end of the subcutaneous conduit may then be coupled to a reducedpressure source. A reduced-pressure delivery conduit may couple firstreduced-pressure interface 528 to a reduced-pressure source. Thereduced-pressure source may be the same for both interfaces, ordifferent reduced-pressure sources may be attached to each interface asdesired.

Referring now primarily to FIG. 9, a dressing assembly 622 having analternative shape is shown. The dressing assembly 622 may be sized andconfigured to apply reduced pressure to different portions of the bodyand may vary in size and shape accordingly. Similarly, the size of thedressing assembly 622 may vary in accordance with the anticipated woundsize. Here, the dressing assembly 622 is shown having many of thefeatures and attributes discussed above, including dressing bolster 624,a first reduced-pressure interface 628, a first reduced-pressure conduit630, a second reduced-pressure interface 632, and a subcutaneousdelivery conduit 634.

In addition to facilitating a pathway for a drain tube, the secondreduced-pressure interface 632 may also function to deliver additionaltreatment and diagnostic applications to the wound site. For example, inaddition to accommodating a drain, the second subcutaneous deliveryconduit 634 may be used to monitor the wound site using a small wiresensor attached to an external diagnostic device. Similarly, the secondreduced-pressure interface 632 may allow for the application ofreduced-pressure therapy at a closely located subcutaneous wound site.In such an application, the subcutaneous delivery conduit 634 can beused to deliver a manifold material to a subcutaneous tissue site suchas bone injury, to which the manifold material and subcutaneous deliveryconduit can be fluidly coupled.

After delivering the manifold material, the subcutaneous delivery tube634 may be coupled to a reduced-pressure source (not shown) to deliverreduced pressure to the subcutaneous tissue site, such as a bone orspinal injury. As such, the addition of the second reduced-pressureinterface 632 provides for the delivery of reduced-pressure therapy totwo distinct tissue sites using a single wound dressing assembly andreduced-pressure source.

Although the present invention and its advantages have been disclosed inthe context of certain illustrative, non-limiting embodiments, it shouldbe understood that various changes, substitutions, permutations, andalterations can be made without departing from the scope of theinvention as defined by the appended claims. It will be appreciated thatany feature that is described in connection to any one embodiment mayalso be applicable to any other embodiment.

It will be understood that the benefits and advantages described abovemay relate to one embodiment or may relate to several embodiments. Itwill further be understood that reference to “an” item refers to one ormore of those items.

The steps of the methods described herein may be carried out in anysuitable order, or simultaneously where appropriate.

Where appropriate, aspects of any of the examples described above may becombined with aspects of any of the other examples described to formfurther examples having comparable or different properties andaddressing the same or different problems.

It will be understood that the above description of preferredembodiments is given by way of example only and that variousmodifications may be made by those skilled in the art. The abovespecification, examples and data provide a complete description of thestructure and use of exemplary embodiments of the invention. Althoughvarious embodiments of the invention have been described above with acertain degree of particularity, or with reference to one or moreindividual embodiments, those skilled in the art could make numerousalterations to the disclosed embodiments without departing from thescope of the claims.

We claim:
 1. A reduced-pressure system, comprising: a dressing bolsteradapted for placing on an epidermis; an over-drape adapted for providinga fluid seal over the dressing bolster and a portion of the epidermis; afirst reduced-pressure interface adapted to be fluidly coupled to thedressing bolster; and a second reduced-pressure interface adapted to becoupled to the over-drape and adapted to be fluidly coupled to thedressing bolster, wherein the second reduced-pressure interface is sizedand configured to receive a subcutaneous delivery conduit and togenerate a compressive force against an outer circumference of thesubcutaneous delivery conduit.
 2. The reduced-pressure system of claim1, further comprising a pre-formed pathway for routing the subcutaneousdelivery conduit through the dressing bolster and the over-drape.
 3. Thereduced-pressure system of claim 1, wherein the second reduced-pressureinterface comprises a nipple with an aperture having an interiordiameter D₁, wherein the subcutaneous delivery conduit has an externaldiameter D₂, and wherein D₁<D₂ whereby the fluid seal is formed.
 4. Thereduced-pressure system of claim 1, wherein the dressing bolster has afirst surface and a second surface for deploying over the epidermis; andfurther comprising: an inner layer having a first surface and a secondsurface, and formed with a treatment-area aperture, and wherein thefirst surface of the inner layer is coupled at least in part to thesecond surface of the dressing bolster, wherein the inner layer ispre-cut to receive the subcutaneous delivery conduit.
 5. Thereduced-pressure system of claim 1, wherein the second reduced-pressureinterface comprises a pliable over-drape and one or more o-rings.
 6. Thereduced-pressure system of claim 1, further comprising: a subcutaneousdelivery conduit comprising a first conduit segment and a second conduitsegment; and wherein the second reduced-pressure interface comprises anadapter that is sized and configured to: receive an end portion of thefirst conduit segment; receive an end portion of the second conduitsegment; and maintain a fluid coupling between the first conduit segmentand the second conduit segment.
 7. The reduced-pressure system of claim1, wherein the second reduced-pressure interface comprises a moldedelastomer having: a first surface; a second surface; an aperture sizedto receive the subcutaneous delivery conduit and to generate thecompressive force against the subcutaneous delivery conduit; and anadhesive for forming a fluid seal between the second surface and theover-drape.
 8. The reduced-pressure system of claim 1, wherein thesecond reduced-pressure interface is sized to transfer a hand-generatedforce equal to an amount of force required to puncture the over-drapewith the subcutaneous delivery conduit.
 9. The reduced-pressure systemof claim 1, further comprising: a reduced-pressure source; and areduced-pressure delivery conduit for fluidly coupling thereduced-pressure source to the first reduced-pressure interface.
 10. Thereduced-pressure system of claim 9, wherein a tissue site is a firsttissue site, the reduced-pressure delivery conduit is a firstreduced-pressure delivery conduit and the reduced-pressure systemfurther comprises: a manifold delivery tube having a passageway and adistal end, the distal end configured to be inserted into thesubcutaneous delivery conduit and placed adjacent a second tissue site;a flowable material deliverable through the manifold delivery tube tothe second tissue site such that the flowable material is capable offilling a void adjacent the second tissue site to create a manifoldhaving a plurality of flow channels in fluid communication with thesecond tissue site; and a second reduced-pressure delivery conduitconfigured for fluid communication with the plurality of flow channelsof the manifold.
 11. The reduced-pressure system of claim 10, whereinthe manifold delivery tube and the second reduced-pressure deliveryconduit are the same tube.
 12. The reduced-pressure system of claim 10,wherein the manifold is bioresorbable.
 13. The reduced-pressure systemof claim 9, further comprising a reduced-pressure indicator fluidlycoupled to the reduced-pressure source.
 14. The reduced-pressure systemof claim 1, wherein the second reduced-pres sure interface comprises amolded elastomer having an aperture sized to receive the subcutaneousdelivery conduit.
 15. The reduced-pressure system of claim 1, whereinthe over-drape is disposed between the dressing bolster and the secondreduced-pressure interface.
 16. The reduced-pressure system of claim 15,wherein the second reduced-pressure interface is configured to reinforcethe over-drape to maintain the fluid seal around a tissue site if theover-drape is breached by the subcutaneous delivery conduit.
 17. A wounddressing assembly comprising: a dressing bolster having a first surfaceand a second surface for deploying over an epidermis; a drape configuredto provide a fluid seal around the dressing bolster with the epidermis,wherein the drape comprises: a first drape portion adapted to bepositioned against the first surface of the dressing bolster, and asecond drape portion adapted to be positioned proximate the secondsurface of the dressing bolster and comprising a treatment-areaaperture; a comfort layer having a first surface and a second surface,and sized to be substantially coextensive with the treatment-areaaperture, and wherein the first surface of the comfort layer is adaptedto be coupled at least in part to the second surface of the dressingbolster; a first reduced-pressure interface configured to be fluidlycoupled to the dressing bolster and operable to receive areduced-pressure supply conduit; and a second reduced-pressureinterface, comprising an interface body formed with an aperture sized toreceive a subcutaneous delivery conduit and to form a fluid seal withthe subcutaneous delivery conduit.
 18. The wound dressing assembly ofclaim 17, wherein the dressing bolster is at least partially pre-cut toallow the subcutaneous delivery conduit to pass to the secondreduced-pressure interface.
 19. The wound dressing assembly of claim 17,wherein the second reduced-pressure interface comprises a pliableover-drape and one or more o-rings.
 20. The wound dressing assembly ofclaim 17, wherein the second reduced-pressure interface is configured togenerate a compressive force against an outer circumference of thesubcutaneous delivery conduit.
 21. The wound dressing assembly of claim17, wherein the interface body comprises a molded elastomer.
 22. Thewound dressing assembly of claim 17, wherein the second reduced-pressureinterface is tapered.
 23. The wound dressing assembly of claim 17,wherein the dressing bolster comprises a plurality of flexibilitynotches.
 24. The wound dressing assembly of claim 17, wherein thedressing bolster further comprises a perforated cylinder of bolstermaterial.
 25. The wound dressing assembly of claim 17, wherein thedressing bolster and the comfort layer are at least partially pre-cut toallow the subcutaneous delivery conduit to pass from the treatment-areaaperture to the second reduced-pressure interface.
 26. The wounddressing assembly of claim 17, wherein the second drape portion furthercomprises an adhesive applied to a first side of the second drapeportion along a perimeter of the treatment-area aperture.
 27. A methodof treating a tissue site, comprising: applying a wound dressingassembly to the tissue site, wherein the wound dressing assemblycomprises: a dressing bolster formed from a medical bolster material andhaving a first side and a second side, an over-drape for providing afluid seal over the dressing bolster and a portion of epidermis, a firstreduced-pressure interface fluidly coupled to the dressing bolster fordelivering reduced-pressure to the dressing bolster, and a secondreduced-pressure interface fluidly coupled to the dressing bolster andhaving an aperture sized to receive a conduit and to generate acompressive force against the conduit; fluidly coupling areduced-pressure delivery conduit to a reduced-pressure source and thefirst reduced-pressure interface; delivering reduced pressure to thereduced-pressure delivery conduit; fluidly coupling a subcutaneousdelivery conduit to the second reduced-pressure interface; anddelivering reduced pressure to the subcutaneous delivery conduit. 28.The method of treating a tissue site of claim 27, wherein the dressingbolster is pre-cut to receive the subcutaneous delivery conduit.
 29. Themethod of treating a tissue site of claim 27, wherein the wound dressingassembly further comprises an inner layer having a first surface and asecond surface, and wherein the first surface of the inner layer isadapted to be coupled at least in part to the second surface of thedressing bolster.
 30. The method of treating a tissue site of claim 27,wherein the tissue site is a first tissue site and further comprising:coupling a manifold delivery tube to the second reduced-pressureinterface, the manifold delivery tube having a passageway and a distalend, the distal end configured to be inserted into the subcutaneousdelivery conduit; delivering a flowable bioresorbable material throughthe manifold delivery tube to a second tissue site such that theflowable bioresorbable material is capable of filling a void adjacentthe second tissue site to create a manifold having a plurality of flowchannels in fluid communication with the second tissue site; coupling areduced-pressure delivery conduit to the second reduced-pressureinterface, the reduced-pressure delivery conduit capable of fluidcommunication with the plurality of flow channels of the manifold; andapplying reduced pressure to the second tissue site.
 31. The method oftreating a tissue site of claim 30, wherein the manifold delivery tubeand the reduced-pressure delivery conduit are the same tube.
 32. Themethod of treating a tissue site of claim 27, wherein the secondreduced-pressure interface comprises a molded elastomer.
 33. The methodof treating a tissue site of claim 27, further comprising inserting asensor attached to an external diagnostic device through the secondreduced-pressure interface to monitor the tissue site.